A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv876069



Internal ID15823339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73841201..74657093hg38UCSC Ensembl
Innerchr17:71837340..72653232hg19UCSC Ensembl
Innerchr17:69348935..70164827hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38815893
hg19815893
hg18815893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576000
Supporting Variants
Samples
Known GenesBTBD17, C17orf77, CD300A, CD300C, CD300E, CD300LB, CD300LD, DNAI2, GPR142, GPRC5C, KIF19, MGC16275, RPL38, TTYH2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv876069
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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